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45922

Supelco

4-Methyl-m-phenylenediamine

analytical standard

Synonym(s):

2,4-Diaminotoluene, 2,4-Toluenediamine, 4-Methyl-1,3-phenylenediamine

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About This Item

Linear Formula:
CH3C6H3(NH2)2
CAS Number:
Molecular Weight:
122.17
Beilstein:
2205839
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

283-285 °C (lit.)

mp

97-99 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

Cc1ccc(N)cc1N

InChI

1S/C7H10N2/c1-5-2-3-6(8)4-7(5)9/h2-4H,8-9H2,1H3

InChI key

VOZKAJLKRJDJLL-UHFFFAOYSA-N

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General description

4-Methyl-m-phenylenediamine is an industrial intermediate, widely used in the production of industrial dyes and polyurethane foams.

Application

4-Methyl-m-phenylenediamine may be used as an analytical reference standard for the quantification of the analyte in biological fluids using high-performance liquid chromatography.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Carc. 1B - Muta. 2 - Repr. 2 - Skin Sens. 1 - STOT RE 2

Target Organs

Liver,Kidney

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

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High-performance liquid chromatography of 2, 6-and 2, 4-diaminotoluene, and its application to the determination of 2, 4-diaminotoluene in urine and plasma.
Unger DP and Friedman AM
Journal of Chromatography A, 174(2), 379-384 (1979)
2,4-Diaminotoluene.
Report on carcinogens : carcinogen profiles, 11, III79-III80 (2004-01-01)
Jeroen A J Vanoirbeek et al.
Toxicological sciences : an official journal of the Society of Toxicology, 109(2), 256-264 (2009-04-01)
Toluene diamine (TDA) is formed when toluene diisocyanate (TDI), a potent sensitizer, comes in contact with an aqueous environment. The sensitizing capacity of TDA and the cross-reactivity between TDI and TDA are unknown. TDA (5-25%) and TDI (0.3%), dissolved in
2,4-Diaminotoluene.
Report on carcinogens : carcinogen profiles, 12, 131-132 (2011-08-19)
Kazunori Narumi et al.
Mutation research, 747(2), 234-239 (2012-06-09)
Various liver micronucleus assay methods, such as those involving partial hepatectomy, treatment with mitogens, and the use of juvenile animals, have been developed. These assays have been proven to be of high sensitivity and specificity to predict hepatocarcinogenicity of compounds

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